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149 results on '"Veldink, J. H."'

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1. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

3. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

7. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

8. Correction for both common and rare cell types in blood is important to identify genes that correlate with age

9. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

10. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

11. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

12. Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR

13. Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR

18. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

20. Associations of autozygosity with a broad range of human phenotypes

21. A SNP panel for identification of DNA and RNA specimens

22. Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults

23. Multicentre, cross-cultural, population-based, case-control study of physical activity as risk factor for amyotrophic lateral sclerosis

24. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

26. Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

27. No association between Borrelia burgdorferi antibodies and amyotrophic lateral sclerosis in a case-control study

29. Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain

30. Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain

31. Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients

34. Van gen naar ziekte; amyotrofische laterale sclerose

37. Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain

38. European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

42. Susceptibility loci for sporadic brain arteriovenous malformation; a replication study and meta-analysis.

44. Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases

47. Multicohort Genomewide Association Study Reveals a New Signal of Protection Against HIV-1 Acquisition

50. Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy

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